Examples of using Cytochrome in English and their translations into Vietnamese
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as compounds in grapefruit affect a number of drugs, including dextromethorphan, through the inhibition of the cytochrome p450 system in the liver,
activation of mitochondrial cytochrome oxide enzyme C,
The main phase II reactions are N-acetylation, glucuronidation and a combination of both.[2][1] Different cytochrome P450 isozymes are involved in the initial steps of human metabolism.
thanks to the presence of myrosinase, an enzyme that activates the cytochrome P 450 isoenzyme in the liver[7].
so hepatic cytochrome P450(CYP) isoenzymes are not involved.[18] The low potential for drug-drug interactions(which could lead to adverse effects) has been suggested as due to this pathway compared to the many common drugs that use the cytochrome P450 metabolic pathway.[2].
ring closures and desaturations.[1][2] Functionally, the αKG-dependent hydroxylases are comparable to cytochrome P450 enzymes, which use oxygen
as compounds in grapefruit affect a number of drugs, including dextromethorphan, through the inhibition of the cytochrome p450 system in the liver,
Single fasting doses are safe and the effects of feeding intake are possibly explained by an interaction between blonanserin and Cytochrome P450 3A4 in the gut.[2].
it is unlikely that there is a pharmacokinetic interaction between smoking(which potently induces certain cytochrome P450 enzymes
Inhibitors and inducers of the cytochrome P450 enzyme CYP3A4 may interact with CPA.[1] Examples of strong CYP3A4 inhibitors include ketoconazole,
as well as the chemical changes of the substance in the body(e.g. by metabolic enzymes such as cytochrome P450 or glucuronosyltransferase enzymes),
trimipramine, and fluoxetine, likely via inactivating cytochrome P450 enzymes.[
the false killer whale and the pilot whales, a study of cytochrome b gene sequences by Richard LeDuc indicated that its closest extant relatives are the snubfin dolphins of the genus Orcaella.[11].
used for Neisseria growth.[10] N. gonorrhoeae is oxidase positive(possessing cytochrome c oxidase)
the release of cytochrome c from mitocondria to cytosol,
stronger and/or longer-lasting opioids, primarily hydromorphone, which is formed in the liver by the cytochrome P450 2D6(CYP2D6) enzyme pathway as well as acetylmorphone.
CoM methyltransferase Hydroxylation of C-5, C-7(followed by transamination), and C-9a.- Likely via cytochrome P450 monooxygenase
Ascorbate has the potential to reduce cytochromes a and c of the respiratory chain as well as molecular oxygen.
NADPH oxidases and cytochromes P450.
Unmediated MFCs emerged in the 1970s; in this type of MFC the bacteria typically have electrochemically active redox proteins such as cytochromes on their outer membrane that can transfer electrons directly to the anode.
